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结核分枝杆菌mRNA干扰酶的特性分析

Characterization of mRNA interferases from Mycobacterium tuberculosis.

作者信息

Zhu Ling, Zhang Yonglong, Teh Jiah-Shin, Zhang Junjie, Connell Nancy, Rubin Harvey, Inouye Masayori

机构信息

Department of Biochemistry, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.

出版信息

J Biol Chem. 2006 Jul 7;281(27):18638-43. doi: 10.1074/jbc.M512693200. Epub 2006 Apr 12.

Abstract

mRNA interferases are sequence-specific endoribonucleases encoded by the toxin-antitoxin systems in the bacterial genomes. MazF from Escherichia coli has been shown to be an mRNA interferase that specifically cleaves at ACA sequences in single-stranded RNAs. It has been shown that MazF induction in E. coli effectively inhibits protein synthesis leading to cell growth arrest in the quasidormant state. Here we have demonstrated that Mycobacterium tuberculosis contains at least seven genes encoding MazF homologues (MazF-mt1 to -mt7), four of which (MazF-mt1, -mt3, -mt4, and -mt6) caused cell growth arrest when induced in E. coli. MazF-mt1 and MazF-mt6 were purified and characterized for their mRNA interferase specificities. We showed that MazF-mt1 preferentially cleaves the era mRNA between U and A in UAC triplet sequences, whereas MazF-mt6 preferentially cleaves U-rich regions in the era mRNA both in vivo and in vitro. These results indicate that M. tuberculosis contains sequence-specific mRNA interferases, which may play a role in the persistent dormancy of this devastating pathogen in human tissues.

摘要

mRNA干扰酶是细菌基因组中毒素-抗毒素系统编码的序列特异性核糖核酸内切酶。来自大肠杆菌的MazF已被证明是一种mRNA干扰酶,它能特异性地切割单链RNA中的ACA序列。研究表明,在大肠杆菌中诱导MazF能有效抑制蛋白质合成,导致细胞生长停滞于准休眠状态。在此我们证明,结核分枝杆菌至少含有7个编码MazF同源物的基因(MazF-mt1至-mt7),其中4个基因(MazF-mt1、-mt3、-mt4和-mt6)在大肠杆菌中诱导表达时会导致细胞生长停滞。对MazF-mt1和MazF-mt6进行了纯化,并对其mRNA干扰酶特异性进行了表征。我们发现,MazF-mt1优先在UAC三联体序列中的U和A之间切割era mRNA,而MazF-mt6在体内和体外均优先切割era mRNA中富含U的区域。这些结果表明,结核分枝杆菌含有序列特异性mRNA干扰酶,这可能在这种破坏性病原体在人体组织中的持续休眠中发挥作用。

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